| Primary Device ID | 00815948020481 | 
| NIH Device Record Key | bf50a27e-5d6a-4cfa-959f-f7870c4144b9 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Indigo | 
| Version Model Number | CATD-C | 
| Company DUNS | 191077671 | 
| Company Name | PENUMBRA, INC. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | Labeling does not contain MRI Safety Information | 
| Human Cell/Tissue Product | false | 
| Device Kit | true | 
| Device Combination Product | false | 
| Single Use | true | 
| Lot Batch | true | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00815948020481 [Primary] | 
| DXE | Catheter, Embolectomy | 
| Steralize Prior To Use | true | 
| Device Is Sterile | true | 
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
[00815948020481]
Ethylene Oxide
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-02-04 | 
| Device Publish Date | 2019-01-03 | 
| 00814548017624 | CATD | 
| 00814548017600 | SEPD | 
| 00815948020481 | Indigo CATD Kit | 
| 00815948022423 | Indigo CATD Kit | 
| 00815948022348 | Aspiration Catheter D Kit | 
| 00815948022331 | Aspiration Catheter D Kit, CE | 
| 00814548019765 | Ind Engine Canister Assembly, CE | 
| 00815948024281 | Indigo CATD Kit |